Literature DB >> 3486769

Differential time course of protection by monoamine oxidase inhibition and uptake inhibition against MPTP neurotoxicity on central catecholamine neurons in mice.

E Sundström, G Jonsson.   

Abstract

Pretreatment with the monoamine oxidase inhibitor pargyline or the catecholamine uptake blocker nomifensine both protected central catecholamine neurons against MPTP-induced neurotoxicity as monitored by analyzing catecholamine levels and [3H]mazindol binding. Post-treatment with the inhibitors showed that the administration of nomifensine could be delayed longer than that of pargyline in order to achieve a protective effect. The results are compatible with the view that the monoamine oxidase-catalyzed conversion of MPTP to a toxic metabolite MPP+ occurs mainly extraneuronally. MPP+ is subsequently taken up and accumulated selectively in catecholamine neurons, initiating degeneration.

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Year:  1986        PMID: 3486769     DOI: 10.1016/0014-2999(86)90113-5

Source DB:  PubMed          Journal:  Eur J Pharmacol        ISSN: 0014-2999            Impact factor:   4.432


  3 in total

1.  Astrocytes as a primary locus for the conversion MPTP into MPP+.

Authors:  W J Brooks; M F Jarvis; G C Wagner
Journal:  J Neural Transm       Date:  1989       Impact factor: 3.575

2.  Evidence for a protective action of the vigilance promoting drug modafinil on the MPTP-induced degeneration of the nigrostriatal dopamine neurons in the black mouse: an immunocytochemical and biochemical analysis.

Authors:  K Fuxe; A M Janson; L Rosén; U B Finnman; S Tanganelli; M Morari; M Goldstein; L F Agnati
Journal:  Exp Brain Res       Date:  1992       Impact factor: 1.972

3.  Attenuation of MPTP-induced dopaminergic neurotoxicity by a serotonin uptake blocker.

Authors:  W J Brooks; M F Jarvis; G C Wagner
Journal:  J Neural Transm       Date:  1988       Impact factor: 3.575

  3 in total

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